Diagnostic and Prognostic Test for Periodontitis and Peri-implantitis (AHC-FRDgrant)
1 other identifier
observational
230
0 countries
N/A
Brief Summary
The dental community, dental insurance companies and the public are becoming increasingly aware of the high prevalence of gum disease around teeth (periodontitis) and around dental implants (peri-implantitis). To date, it cannot be accurately predicted which individuals will develop or re-develop periodontitis or peri-implantitis, leading most dental patients to undergo unnecessary treatment and undue risks and costs. Gingival fluid is a serum-like fluid that diffuses into the oral cavity by flowing between the gum and the tooth or dental implant. Oral bacteria that grow around teeth and dental implants induce inflammation and change the amount and composition of the gingival fluid. The study hypothesizes that the spectra of metabolites in the inflammatory transudates and exudates around teeth and dental-implants are predictors of future periodontitis or peri-implantitis. The first objective is to use proton nuclear magnetic resonance (H-NMR) spectroscopy in a cross-sectional study to map mapping the metabolites in the gingival fluid that are capable of discriminating between healthy gum tissue and gum tissue that shows signs of periodontitis or dental peri-implantitis. The second objective is to begin prospective measurement of gingival fluid metabolites every 6 months in (i) individuals without periodontitis or peri-implantitis (healthy group), (ii) individuals with periodontitis or peri- implantitis who have been informed of the need for treatment - but have decided not to have treatment (untreated group) and (iii) individuals who received treatment for periodontitis or peri-implantitis and are now receiving regular dental hygiene care every 3 months (high risk group). By defining metabolites that can discriminate health from disease (Aim 1) and by measuring proportional changes of key metabolites relative to disease progression over time (Aim 2), the study will be able to predict in a site-specific manner, (a) the risk of disease initiation in people who do not initially have periodontitis or peri-implantitis (healthy persons), and (b) disease progression in untreated people or in people who were treated and are currently in a dental hygiene maintenance program. Accomplishing these two aims will provide a foundation from which to increase the efficacy of prevention whilst abating the morbidity and cost associated with current clinical practice.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2016
Longer than P75 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 5, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 29, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 29, 2024
CompletedFirst Submitted
Initial submission to the registry
January 14, 2025
CompletedFirst Posted
Study publicly available on registry
January 20, 2025
CompletedJanuary 20, 2025
January 1, 2025
7.2 years
January 14, 2025
January 14, 2025
Conditions
Outcome Measures
Primary Outcomes (2)
defining metabolites that can discriminate health from disease
Gingival fluid samples using use proton nuclear magnetic resonance (H-NMR) spectroscopy, every 6 months for 24 months
6, 12, 18, 24 months
measuring proportional changes of key metabolites relative to disease progression over time
Gingival fluid samples using use proton nuclear magnetic resonance (H-NMR) spectroscopy, every 6 months for 24 months
6, 12, 18, 24 months
Study Arms (3)
Healthy group
individuals without periodontitis or peri-implantitis
untreated group
individuals with periodontitis or peri- implantitis who have been informed of the need for treatment - but have decided not to have treatment (untreated group)
high risk group
individuals who received treatment for periodontitis or peri-implantitis and are now receiving regular dental hygiene care every 3 months (high risk group).
Interventions
Eligibility Criteria
Subjects with disease (cases) were diagnosed with generalized chronic severe periodontitis with at least five teeth having clinical evidence of disease \[clinical attachment loss (CAL) ≥ 5mm and at least one site with probing depth (PD) ≥ 7 mm\], and radiographic evidence of at least 30% bone loss. Control subjects exhibited a healthy periodontium (no PD \>3 mm. no site with CAL) with no radiographic evidence of bone loss. Case and control subjects were in good general health. Smoking habits were noted. Case and control exclusion criteria included: 1) uncontrolled systemic disease, such as diabetes; 2) systemic antibiotic use within the past 3 months; 3) unable to provide consent; and 4) history of periodontal treatment or local antibiotic use in the past 12 months; 5) use of NSAIDs in the past 3 weeks.
You may qualify if:
- Subjects with disease (cases) were diagnosed with generalized chronic severe periodontitis with at least five teeth having clinical evidence of disease \[clinical attachment loss (CAL) ≥ 5mm, at least one site with probing depth (PD) ≥ 7 mm\] and radiographic evidence of at least 30% bone loss
- Control subjects exhibited a healthy periodontium (no PD \>3 mm. no site with CAL) with no radiographic evidence of bone loss.
- Case and control subjects were in good general health.
You may not qualify if:
- uncontrolled systemic disease, such as diabetes;
- systemic antibiotic use within the past 3 months;
- unable to provide consent; and
- history of periodontal treatment or local antibiotic use in the past 12 months;
- use of NSAIDs in the past 3 weeks.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Biospecimen
gingival fluid
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 14, 2025
First Posted
January 20, 2025
Study Start
December 5, 2016
Primary Completion
January 29, 2024
Study Completion
January 29, 2024
Last Updated
January 20, 2025
Record last verified: 2025-01